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ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
medimedia.ir
Cerebral palsy: Classification and clinical features
Cerebral palsy: Epidemiology, etiology, and prevention
Cerebral palsy: Evaluation and diagnosis
Cerebral palsy: Overview of management and prognosis
Cerebral palsy: Treatment of spasticity, dystonia, and associated orthopedic issues
Acute stroke (ischemic and hemorrhagic) in children and adults with sickle cell disease
Cerebral venous thrombosis: Etiology, clinical features, and diagnosis
Cerebral venous thrombosis: Treatment and prognosis
Clinical manifestations and diagnosis of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome)
Hemorrhagic stroke in children
Hereditary hemorrhagic telangiectasia (HHT): Evaluation and therapy for specific vascular lesions
Hereditary hemorrhagic telangiectasia (HHT): Routine care including screening for asymptomatic AVMs
Ischemic stroke in children and young adults: Epidemiology, etiology, and risk factors
Ischemic stroke in children: Clinical presentation, evaluation, and diagnosis
Ischemic stroke in children: Management and prognosis
Moyamoya disease and moyamoya syndrome: Etiology, clinical features, and diagnosis
Moyamoya disease and moyamoya syndrome: Treatment and prognosis
Stroke in the newborn: Classification, manifestations, and diagnosis
Stroke in the newborn: Management and prognosis
Vascular malformations of the central nervous system
Acute disseminated encephalomyelitis (ADEM) in children: Pathogenesis, clinical features, and diagnosis
Acute disseminated encephalomyelitis (ADEM) in children: Treatment and prognosis
Alexander disease
Cerebrotendinous xanthomatosis
Clinical presentation, course, and prognosis of multiple sclerosis in adults
Differential diagnosis of acute central nervous system demyelination in children
Disease-modifying therapies for multiple sclerosis: Pharmacology, administration, and adverse effects
Neuromyelitis optica spectrum disorders (NMOSD): Clinical features and diagnosis
Neuromyelitis optica spectrum disorders (NMOSD): Treatment and prognosis
Optic neuritis: Pathophysiology, clinical features, and diagnosis
Optic neuritis: Prognosis and treatment
Pathogenesis, clinical features, and diagnosis of pediatric multiple sclerosis
Pelizaeus-Merzbacher disease
Sjögren-Larsson syndrome
Treatment and prognosis of pediatric multiple sclerosis
Vanishing white matter disease
Attention deficit hyperactivity disorder in children and adolescents: Clinical features and diagnosis
Attention deficit hyperactivity disorder in children and adolescents: Overview of treatment and prognosis
Autism spectrum disorder in children and adolescents: Behavioral and educational interventions
Autism spectrum disorder in children and adolescents: Clinical features
Autism spectrum disorder in children and adolescents: Complementary and alternative therapies
Autism spectrum disorder in children and adolescents: Evaluation and diagnosis
Autism spectrum disorder in children and adolescents: Overview of management
Autism spectrum disorder in children and adolescents: Pharmacologic interventions
Cerebral palsy: Classification and clinical features
Intellectual disability (ID) in children: Clinical features, evaluation, and diagnosis
Intellectual disability (ID) in children: Management, outcomes, and prevention
Intellectual disability in children: Evaluation for a cause
Specific learning disorders in children: Clinical features
Specific learning disorders in children: Educational management
Specific learning disorders in children: Evaluation
Specific learning disorders in children: Role of the primary care provider
Acute disseminated encephalomyelitis (ADEM) in children: Pathogenesis, clinical features, and diagnosis
Acute toxic-metabolic encephalopathy in children
Clinical features, diagnosis, and treatment of neonatal encephalopathy
Etiology and pathogenesis of neonatal encephalopathy
Approach to the infant with hypotonia and weakness
Detailed neurologic assessment of infants and children
Diagnosis of brain death
Evaluation of stupor and coma in children
Lumbar puncture: Indications, contraindications, technique, and complications in children
Macrocephaly in infants and children: Etiology and evaluation
Treatment and prognosis of coma in children
Ketogenic dietary therapies for the treatment of epilepsy
Clinical manifestations and diagnosis of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome)
Fabry disease: Neurologic manifestations
Hereditary hemorrhagic telangiectasia (HHT): Evaluation and therapy for specific vascular lesions
Hereditary hemorrhagic telangiectasia (HHT): Routine care including screening for asymptomatic AVMs
Huntington disease: Genetics and pathogenesis
Krabbe disease
Metachromatic leukodystrophy
Mitochondrial disorders: Treatment
Mitochondrial myopathies: Clinical features and diagnosis
Mitochondrial structure, function, and genetics
Mucopolysaccharidoses: Clinical features and diagnosis
Mucopolysaccharidoses: Complications
Mucopolysaccharidoses: Treatment
Neuronal ceroid lipofuscinosis
Organic acidemias: An overview and specific defects
Overview of Niemann-Pick disease
Peroxisomal disorders
Rett syndrome: Genetics, clinical features, and diagnosis
Rett syndrome: Treatment and prognosis
Spinal muscular atrophy
Sturge-Weber syndrome
The genodermatoses: An overview
Tuberous sclerosis complex: Genetics, clinical features, and diagnosis
Tuberous sclerosis complex: Management and prognosis
Vascular malformations of the central nervous system
Wilson disease: Diagnostic tests
Wilson disease: Treatment and prognosis
X-linked adrenoleukodystrophy and adrenomyeloneuropathy
Acute treatment of migraine in children
Cold stimulus headache
Cyclic vomiting syndrome
Elevated intracranial pressure (ICP) in children: Clinical manifestations and diagnosis
Headache in children: Approach to evaluation and general management strategies
Migraine with brainstem aura
Pathophysiology, clinical features, and diagnosis of migraine in children
Preventive treatment of migraine in children
Tension-type headache in children
Types of migraine and related syndromes in children
Vestibular migraine
Acute viral encephalitis in children: Clinical manifestations and diagnosis
Acute viral encephalitis in children: Treatment and prevention
Clinical manifestations and diagnosis of Rocky Mountain spotted fever
Viral meningitis in children: Clinical features and diagnosis
Anencephaly
Chiari malformations
Closed spinal dysraphism: Clinical manifestations, diagnosis, and management
Closed spinal dysraphism: Pathogenesis and types
Hydrocephalus in children: Clinical features and diagnosis
Hydrocephalus in children: Management and prognosis
Hydrocephalus in children: Physiology, pathogenesis, and etiology
Myelomeningocele (spina bifida): Anatomy, clinical manifestations, and complications
Myelomeningocele (spina bifida): Management and outcome
Myelomeningocele (spina bifida): Orthopedic issues
Myelomeningocele (spina bifida): Urinary tract complications
Primary (congenital) encephalocele
Cyclic vomiting syndrome
Idiopathic intracranial hypertension (pseudotumor cerebri): Clinical features and diagnosis
Idiopathic intracranial hypertension (pseudotumor cerebri): Epidemiology and pathogenesis
Idiopathic intracranial hypertension (pseudotumor cerebri): Prognosis and treatment
Pathogenesis, clinical features, and diagnosis of pediatric multiple sclerosis
Acquired torticollis in children
Acute cerebellar ataxia in children
Ataxia-telangiectasia
Autosomal dominant spinocerebellar ataxias
Bradykinetic movement disorders in children
Congenital muscular torticollis: Clinical features and diagnosis
Congenital muscular torticollis: Management and prognosis
Friedreich ataxia
Hyperkinetic movement disorders in children
Overview of the hereditary ataxias
Sydenham chorea
Tourette syndrome: Management
Tourette syndrome: Pathogenesis, clinical features, and diagnosis
Wilson disease: Clinical manifestations, diagnosis, and natural history
Wilson disease: Epidemiology and pathogenesis
Brachial plexus syndromes
Clinical features, evaluation, and diagnosis of neonatal seizures
Congenital myopathies
Etiology and pathogenesis of neonatal encephalopathy
Etiology and prognosis of neonatal seizures
Germinal matrix hemorrhage and intraventricular hemorrhage (GMH-IVH) in the newborn: Pathogenesis, clinical presentation, and diagnosis
Germinal matrix hemorrhage and intraventricular hemorrhage (GMH-IVH) in the newborn: Prevention, management, and complications
Neonatal brachial plexus palsy
Neonatal cerebellar hemorrhage
Neuromuscular junction disorders in newborns and infants
Overview of cerebellar injury and malformations in neonates
Overview of infantile epilepsy syndromes
Overview of neonatal brain malformations of the cortex
Overview of neonatal epilepsy syndromes
Overview of peripheral nerve and muscle disorders causing hypotonia in the newborn
Stroke in the newborn: Classification, manifestations, and diagnosis
Stroke in the newborn: Management and prognosis
Treatment of neonatal seizures
Neurofibromatosis type 1 (NF1): Management and prognosis
Neurofibromatosis type 1 (NF1): Pathogenesis, clinical features, and diagnosis
Sturge-Weber syndrome
Tuberous sclerosis complex: Genetics, clinical features, and diagnosis
Tuberous sclerosis complex: Management and prognosis
Acute flaccid myelitis
Approach to the metabolic myopathies
Duchenne and Becker muscular dystrophy: Clinical features and diagnosis
Duchenne and Becker muscular dystrophy: Genetics and pathogenesis
Duchenne and Becker muscular dystrophy: Glucocorticoid and disease-modifying treatment
Duchenne and Becker muscular dystrophy: Management and prognosis
Emery-Dreifuss muscular dystrophy
Energy metabolism in muscle
Facioscapulohumeral muscular dystrophy
Guillain-Barré syndrome in children: Epidemiology, clinical features, and diagnosis
Guillain-Barré syndrome in children: Treatment and prognosis
Hereditary spastic paraplegia
Juvenile dermatomyositis and polymyositis: Epidemiology, pathogenesis, and clinical manifestations
Juvenile dermatomyositis and polymyositis: Treatment, complications, and prognosis
Limb-girdle muscular dystrophy
Metabolic myopathies caused by disorders of lipid and purine metabolism
Myotonic dystrophy: Etiology, clinical features, and diagnosis
Myotonic dystrophy: Treatment and prognosis
Neonatal brachial plexus palsy
Neuromuscular junction disorders in newborns and infants
Oculopharyngeal, distal, and congenital muscular dystrophies
Pathogenesis of myasthenia gravis
Patient education: Overview of muscular dystrophies (Beyond the Basics)
Spinal muscular atrophy
Charcot-Marie-Tooth disease: Genetics, clinical features, and diagnosis
Charcot-Marie-Tooth disease: Management and prognosis
Fabry disease: Neurologic manifestations
Facial nerve palsy in children
Hereditary sensory and autonomic neuropathies
Krabbe disease
Metachromatic leukodystrophy
Neuropathies associated with hereditary disorders
Overview of Niemann-Pick disease
Overview of acquired peripheral neuropathies in children
Overview of hereditary neuropathies
Fourth cranial nerve (trochlear nerve) palsy
Horner syndrome
Myopathies affecting the extraocular muscles in children
Ocular gaze disorders
Optic neuritis: Pathophysiology, clinical features, and diagnosis
Optic neuritis: Prognosis and treatment
Pendular nystagmus
Sixth cranial nerve (abducens nerve) palsy
Third cranial nerve (oculomotor nerve) palsy in children
Antiseizure medications: Mechanism of action, pharmacology, and adverse effects
Benign (self-limited) focal epilepsies of childhood
Childhood absence epilepsy
Clinical features and complications of status epilepticus in children
Clinical features and evaluation of febrile seizures
Clinical features, evaluation, and diagnosis of neonatal seizures
Dravet syndrome: Management and prognosis
Epilepsy in children: Comorbidities, complications, and outcomes
Epilepsy syndromes in children
Etiology and prognosis of neonatal seizures
Focal epilepsy: Causes and clinical features
Infantile epileptic spasms syndrome: Clinical features and diagnosis
Infantile epileptic spasms syndrome: Etiology and pathogenesis
Infantile epileptic spasms syndrome: Management and prognosis
Juvenile myoclonic epilepsy
Lennox-Gastaut syndrome
Management of convulsive status epilepticus in children
Nonepileptic paroxysmal disorders in children
Nonepileptic paroxysmal disorders in infancy
Overview of infantile epilepsy syndromes
Overview of neonatal epilepsy syndromes
Psychogenic nonepileptic seizures: Management and prognosis
Seizures and epilepsy in children: Classification, etiology, and clinical features
Seizures and epilepsy in children: Clinical and laboratory diagnosis
Seizures and epilepsy in children: Initial treatment and monitoring
Seizures and epilepsy in children: Refractory seizures
Treatment and prognosis of febrile seizures
Treatment of neonatal seizures
Vagus nerve stimulation therapy for the treatment of epilepsy
Child abuse: Epidemiology, mechanisms, and types of abusive head trauma in infants and children
Child abuse: Evaluation and diagnosis of abusive head trauma in infants and children
Intracranial epidural hematoma in children: Clinical features, diagnosis, and management
Intracranial epidural hematoma in children: Epidemiology, anatomy, and pathophysiology
Intracranial subdural hematoma in children: Clinical features, evaluation, and management
Intracranial subdural hematoma in children: Epidemiology, anatomy, and pathophysiology
Minor blunt head trauma in infants and young children (<2 years): Clinical features and evaluation

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